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| Product | Description | |
|---|---|---|
| Penciclovir (2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one) | An antiviral. Group: Biochemicals. Alternative Names: 2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. |  Worldwide |
| Penciclovir-d4 | Penciclovir-d4 is the deuterium labeled Penciclovir. Penciclovir is reported to be potent against HSV types 1 and 2 with IC50 of 0.04-1.8 μg/mL and 0.06-4.4 μg/mL, respectively. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one. Product Category: Inhibitors. Appearance: White Solid. CAS No. 1020719-72-5. Molecular formula: C10H11D4N5O3. Mole weight: 257.28. Purity: 0.96. IUPACName: 2-amino-9-[1,1,2,2-tetradeuterio-4-hydroxy-3-(hydroxymethyl)butyl]-3H-purin-6-one. Canonical SMILES: C1=NC2=C(N1CCC(CO)CO)NC(=NC2=O)N. Product ID: ACM1020719725. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Penciclovir-[d4] | Penciclovir-[d4] is the labelled analogue of Penciclovir, which is a guanosine analogue antiviral drug used for the treatment of various herpesvirusinfections. Synonyms: Penciclovir D4. Grade: 95% by HPLC; 95% atom D. CAS No. 1020719-72-5. Molecular formula: C10H11D4N5O3. Mole weight: 257.28. |  |
| Penciclovir-d4 (2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one) | A deuterated version of Penciclovir, an antiviral. Group: Biochemicals. Alternative Names: 2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Penconazole | Penconazole. Group: Biochemicals. Alternative Names: (±)-Penconazole; CGA 71818; Ofir; Omnex; Omnex WP 10; Pine gel; Regal gel; Topas; Topas (fungicide); Topaze. Grades: Highly Purified. CAS No. 66246-88-6. Pack Sizes: 500mg. Molecular Formula: C13H15Cl2N3, Molecular Weight: 284.18. US Biological Life Sciences. | Worldwide |
| Penconazole-d5 | Penconazole-d5. Group: Biochemicals. Alternative Names: (±)-Penconazole-d5; CGA 71818-d5; Ofir-d5; Omnex-d5; Topas-d5. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C13H10D5Cl2N3, Molecular Weight: 289.22. US Biological Life Sciences. | Worldwide |
| Pencycuron | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. |  |
| Pencycuron | Pencycuron. Group: Biochemicals. Alternative Names: Monceraen 250SC; Monceren; NTN 19701; N-[(4-chlorophenyl)methyl]-N-cyclopentyl-N'-phenylurea. Grades: Highly Purified. CAS No. 66063-05-6. Pack Sizes: 250mg. Molecular Formula: C19H21ClN2O, Molecular Weight: 328.84. US Biological Life Sciences. | Worldwide |
| Pendimethalin | 1g Pack Size. Group: Analytical Reagents, Building Blocks, Organics. Formula: C13H19N3O4. CAS No. 40487-42-1. Prepack ID 90026283-1g. Molecular Weight 281.31. See USA prepack pricing. |  |
| Pendimethalin | Herbicide used to control the spread of weedgrass. Group: Biochemicals. Alternative Names: N-(1-Ethylpropyl)-3,4-dimethyl-2,6-dinitro-benzenamine; 3,4-Dimethyl-2,6-dinitro-N-(1-ethylpropyl)aniline; Accotab; Acumen; Herbadox; Most Micro; N-(1-Ethylpropyl)-2,6-dinitro-3,4-xylidine; Pendimax; Stomp; Phenoxalin; Prowl. Grades: Highly Purified. CAS No. 40487-42-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Pendimethalin | Pendimethalin is an orally active herbicide that controls annual grasses and certain broadleaf weeds. Pendimethalin induces Apoptotic cell death through activating ER stress-mediated mitochondrial dysfunction in human umbilical vein endothelial cells [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 40487-42-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B0862. |  |
| Pendimethalin-d5 | Pendimethalin-d5. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-(1-Ethylpropyl)-3,4-dimethyl-2,6-dinitro-benzenamine-d5; 3,4-Dimethyl-2,6-dinitro-N-(1-ethylpropyl)aniline-d5; Accotab-d5; Acumen-d5; Herbadox-d5; Most Micro-d5; N-(1-Ethylpropyl)-2,6-dinitro-3,4-xylidine-d5; Pendimax-d5; Stomp-d5; Phenoxalin-d5; Prowl-d5. Product Category: Heterocyclic Organic Compound. CAS No. 1219803-39-0. Molecular formula: C13H14D5N3O4. Mole weight: 286.34. Purity: 98 atom % D. IUPACName: 3,4-dimethyl-2,6-dinitro-N-(2,2,3,4,4-pentadeuteriopentan-3-yl)aniline. Canonical SMILES: CCC(CC)NC1=C(C=C(C(=C1[N+](=O)[O-])C)C)[N+](=O)[O-]. Product ID: ACM1219803390. Alfa Chemistry ISO 9001:2015 Certified. | |
| Pendimethalin-[d5] | Pendimethalin-[d5] is the labelled analogue of Pendimethalin. Pendimethalin is an herbicide used to control annual grasses and certain broadleaf weeds. Synonyms: Pendimethalin D5. Grade: 95% by HPLC; 95% atom D. CAS No. 1219803-39-0. Molecular formula: C13H14D5N3O4. Mole weight: 286.34. | |
| Penduletin | Penduletin is isolated from the leaves of Laggera pterodonta. It significantly reduces the production of TGF-β1, and has strong activity against EV71 who has low cytotoxicity in vitro. Uses: Antiviral; antitumor cells activity. Synonyms: 3,6,7-Trimethyl-6-hydroxykaempferol. Grade: 98%. CAS No. 569-80-2. Molecular formula: C18H16O7. Mole weight: 344.3. | |
| Penehyclidine Hydrochloride | Penehyclidine Hydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 151937-76-7. Molecular formula: C20H30ClNO2. Mole weight: 351.91. Catalog: APB151937767. | |
| Penehyclidine Impurity 3 | Penehyclidine Impurity 3. Uses: For analytical and research use. Group: Impurity standards. CAS No. 151673-92-6. Molecular formula: C13H16O. Mole weight: 188.27. Catalog: APB151673926. | |
| Penehyclidine Intermediate A | Penehyclidine Intermediate A. Uses: For analytical and research use. Group: Impurity standards. CAS No. 151673-91-5. Molecular formula: C13H18O2. Mole weight: 206.29. Catalog: APB151673915. | |
| Penethamate | Penethamate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Penethamate;penethamate hydroiodide;Penethacillin;PENICILLINGDIETHYLAMINOETHYLESTER;(2S,5β)-3,3-Dimethyl-7-oxo-6α-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid 2-(diethylamino)ethyl ester;(6α-[(Phenylacetyl)amino]penicillanic acid 2-(diethylamino)ethyl) ester. CAS No. 3689-73-4. Molecular formula: C22H31N3O4S. Mole weight: 433.57. Purity: 0.96. IUPACName: 2-(diethylamino)ethyl(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Canonical SMILES: CCN(CC)CCOC(=O)C1C(SC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)(C)C. Density: 1.24g/cm³. Product ID: ACM3689734. Alfa Chemistry ISO 9001:2015 Certified. | |
| Penetran Cl | Synthetic, an inhibitor of high-affinity choline uptake (HAChU) in synaptosomes. Grade: ≥ 98%.(TLC). Molecular formula: C14H14NOCl.HCl. Mole weight: 284.18. | |
| Penetratin | The first 16 amino acids of Penetratin are derived from the third helix of the Antennapedia protein homeodomain, known as the protein transduction domain (PTD). Penetratin linked to phosphodiester oligonucleotides can penetrate neuronal cell membranes and down-regulate genes. It contains a nuclear localization sequence that facilitates internalization of cargo into living cells. Uses: Penetratin, also known as antennapedia homeodomain or penetratin-1, is a cell-penetrating peptide derived from the drosophila antennapedia protein. this short peptide sequence, consisting of 16 amino acids (rqikiwfqnrrmkwkk), has attracted great attention in the biotechnology and medical fields due to its outstanding ability to penetrate cell membranes and deliver a variety of cargo molecules into. Synonyms: H-Arg-Gln-Ile-Lys-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Lys-Trp-Lys-Lys-NH2. Grade: >98%. CAS No. 214556-79-3. Molecular formula: C104H169N35O19S. Mole weight: 2245.78. | |
| Penetratin | Penetratin is a peptide derived from the amphiphilic Drosophila Antennapedia homeodomain [1]. Uses: Scientific research. Group: Peptides. CAS No. 940866-75-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P2529. | |
| Penetratin-Arg | Penetratin-Arg, a cell-penetrating peptide (CPP) derived from the 3rd helix of Drosophila Antennapedia homeodomain protein, can permeate cell membrane at low micromolar concentration without significantly affecting membrane. It contains a nuclear localization sequence that facilitates internalization of cargo into living cells. Synonyms: PenArg; H-Arg-Gln-Ile-Arg-Ile-Trp-Phe-Gln-Asn-Arg-Arg-Met-Arg-Trp-Arg-Arg-NH2; L-arginyl-L-glutaminyl-L-isoleucyl-L-arginyl-L-isoleucyl-L-tryptophyl-L-phenylalanyl-L-glutaminyl-L-asparagyl-L-arginyl-L-arginyl-L-methionyl-L-arginyl-L-tryptophyl-L-arginyl-L-argininamide. Grade: >98%. Molecular formula: C104H169N43O19S. Mole weight: 2357.80. | |
| Penetratin-eiF4E | Penetratin-eiF4E. Synonyms: (D-Arg)-(D-Gln)-(D-Ile)-(D-Lys)-(D-Ile)-(D-Trp)-(D-Phe)-(D-Gln)-(D-Asn)-(D-Arg)-(D-Arg)-(D-Met)-(D-Lys)-(D-Trp)-(D-Lys)-(D-Lys)-Ile-Gly-Tyr-Gln-Ser-His-Ala-Asp-Thr-Ala-Thr-Lys-Ser-Gly-Ser-Thr-Thr-Lys-Asn-Arg-Phe-Val-Val. Molecular formula: C215H344N66O57S. Mole weight: 4797.78. | |
| Penetratin Trifluoroacetate | Penetratin, a cell-penetrating peptide (CPP), is renowned for its ability to facilitate the intracellular delivery of various bioactive molecules, including proteins, peptides, nucleic acids, and nanoparticles, across the cell membrane. It shows antimicrobial and antifungal activity. Grade: 98%. Molecular formula: C106H170F3N35O21S. Mole weight: 2359.80. | |
| Penflufen | Penflufen is a highly efficient, broad-spectrum succinate dehydrogenase inhibitor (SDHI). Penflufen can be used as a fungicide and has broad bioactivity against many fungal diseases, including potato black scurf, wheat sharp eyespot, rice sheath blight, and root rot in peanut and other similar fungal diseases [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 494793-67-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139161. | |
| Penflufen | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. Alternative Names: 5-Fluoro-1,3-dimethyl-N-[2-(1,3-dimethylbutyl)phenyl]-1H-pyrazole-4-carboxamide,N-[2-(1,3-Dimethylbutyl)phenyl]-5-fluoro-1,3-dimethyl-1H-pyrazole-4-carboxamide, Emesto, N-[2-(1,3-Dimethylbutyl)phenyl]-1,3-dimethyl-5-fluoro-1H-pyrazole-4-carboxamide, Penflufen, Pyflufen, Cerenturf Forte. | |
| Penfluridol | Penfluridol. Group: Biochemicals. Grades: Highly Purified. CAS No. 26864-56-2. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Penfluridol | Penfluridol (R-16341) is a potent, long-acting, first-generation, oral diphenylbutylpiperidine antipsychotic agent by targeting D2-like dopamine receptor. Penfluridol effectively inhibits TNFα-induced NF-κB activation and alleviates the severity of arthritis and colitis in vivo. Penfluridol is a Ca 2+ -calmodulin inhibitor. Penfluridol induces apoptosis and autophagy. Penfluridol is used for chronic schizophrenia, acute psychosis, Tourette syndrome and autoimmune diseases. Penfluridol inhibites the growth of E. faecalis planktonic cells with the MIC of 7.81 μg/ml [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: R-16341. CAS No. 26864-56-2. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-B1077. | |
| Penguin AvBD103a | Penguin AvBD103a is an antimicrobial peptide found in King Penguin stomach, Aptenodytes patagonicus, and has anti-gram-positive bacteria, gram-negative bacteria and fungal activity. Synonyms: Spheniscin 1; Penguin avian β-defensin 103a; Sphe-1; defensin pBD-1 (King penguin); L-Tryptophan, L-seryl-L-phenylalanylglycyl-L-leucyl-L-cysteinyl-L-arginyl-L-leucyl-L-arginyl-L-arginylglycyl-L-phenylalanyl-L-cysteinyl-L-alanyl-L-histidylglycyl-L-arginyl-L-cysteinyl-L-arginyl-L-phenylalanyl-L-prolyl-L-seryl-L-isoleucyl-L-prolyl-L-isoleucylglycyl-L-arginyl-L-cysteinyl-L-seryl-L-arginyl-L-phenylalanyl-L-valyl-L-glutaminyl-L-cysteinyl-L-cysteinyl-L-arginyl-L-arginyl-L-valyl-, cyclic(5→33),(12→27),(17→34)-tris(disulfide). Grade: >85%. CAS No. 641144-91-4. | |
| Penguin AvBD103b | Penguin AvBD103b is an antimicrobial peptide found in King Penguin stomach, Aptenodytes patagonicus, and has antibacterial activity. Synonyms: Spheniscin 2; Penguin avian β-defensin 103b; Sphe-1; defensin pBD-2 (King penguin); L-Tryptophan, L-seryl-L-phenylalanylglycyl-L-leucyl-L-cysteinyl-L-arginyl-L-leucyl-L-arginyl-L-arginylglycyl-L-phenylalanyl-L-cysteinyl-L-alanyl-L-arginylglycyl-L-arginyl-L-cysteinyl-L-arginyl-L-phenylalanyl-L-prolyl-L-seryl-L-isoleucyl-L-prolyl-L-isoleucylglycyl-L-arginyl-L-cysteinyl-L-seryl-L-arginyl-L-phenylalanyl-L-valyl-L-glutaminyl-L-cysteinyl-L-cysteinyl-L-arginyl-L-arginyl-L-valyl-, cyclic(5→33),(12→27),(17→34)-tris(disulfide). Grade: >85%. CAS No. 641144-92-5. | |
| Penicillamine | Penicillamine (D-(-)-Penicillamine) is a penicillin metabolic degradation product, can be used as a heavy metal chelator. Penicillamine reduces free copper and reduces oxidative stress. Penicillamine has effect of seizures through nitric oxide/NMDA pathways. Penicillamine is a potential immune modulator. Penicillamine can be used for the research of Wilson disease, rheumatoid arthritis, and cystinuria [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: D-(-)-Penicillamine. CAS No. 52-67-5. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-B0300. | |
| Penicillamine | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Mercaptyl, 2-Amino-3-mercapto-3-methylbutanoic acid, Penicillamin, Kuprenil, DPA, NSC 81549, (2S)-2-Amino-3-methyl-3-sulfanylbutanoic acid, D-Mercaptovaline, Cuprenil, ?-Thiovaline, Cupripen,Penicillamine, (S)-3,3-Dimethylcysteine, (2S)-2-Amino-3-methyl-3-sulfanylbutanoic acid, Cuprimine, D-Valine, 3-mercapto-, D-(-)-Penicillamine, D-3-Mercaptovaline, D-Penamine, Reduced D-penicillamine, Depen, Valine, 3-mercapto-, D- (8CI), D-Penicillamine, Penicillamine, (S)-Penicillamine, Metalcaptase, Pendramine, Sufirtan, (-)-Penicillamine, Artamin, Reduced penicillamine, Depamine, Trolovol, Perdolat. | |
| Penicillamine | Penicillamine is used as an antirheumatic and as a chelating agent in Wilson's disease. Synonyms: Dimethyl Cysteine. Grade: >98%. CAS No. 52-67-5. Molecular formula: C5H11NO2S. Mole weight: 149.21. | |
| Penicillamine disulfide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Oxidized penicillamine, Penicillamine disulfide, Oxidized D-penicillamine, D-Penicillamine disulfide,D-Valine, 3,3'-dithiobis-, Valine, 3,3'-dithiodi-, D- (8CI), NSC 87505. | |
| Penicillanyl Ampicillinamide | Penicillanyl Ampicillinamide. Uses: For analytical and research use. Group: Impurity standards. Catalog: APS002737. Format: Neat. | |
| Penicillic acid | Penicillic acid is a polyketide mycotoxin produced by several species of Aspergillus and Penicillium. Penicillic acid exhibits cytotoxicity in rat alveolar macrophages (AM) in vitro. Penicillic acid inhibits Fas ligand-induced apoptosis by blocking self-processing of caspase-8. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2,5-Hexadienoic acid, 3-methoxy-5-methyl-4-oxo-. Product Category: Inhibitors. Appearance: Solid. CAS No. 90-65-3. Molecular formula: C8H10O4. Mole weight: 170.16. Purity: 0.9954. Canonical SMILES: C=C(C)C(/C(OC)=C/C(O)=O)=O. Product ID: ACM90653-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Penicillic acid | Penicillic acid is a polyketide mycotoxin produced by several species of Aspergillus and Penicillium. Penicillic acid exhibits cytotoxicity in rat alveolar macrophages (AM) in vitro. Penicillic acid inhibits Fas ligand-induced apoptosis by blocking self-processing of caspase-8 [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 90-65-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N6777. | |
| Penicillic acid | It is produced by the strain of Pen. puberulum. It is an antibiotic with activity against gram-positive bacteria, negative bacteria and mycobacterium. It is also used as a raw material for various semisynthetic penicillins. Penicillic acid, a kind of polyketide mycotoxin, has been found to restrain GDP-mannose dehydrogenase and sorts of other dehydrogenases. It causes DNA to break. Synonyms: 3-Methoxy-5-methyl-4-oxohexa-2,5-dienoic acid; Penicillinsaure; NSC 402844; γ-Keto-β-methoxy-δ-methylene-Δα-hexenoic Acid; HSDB 3523. Grade: 98%. CAS No. 90-65-3. Molecular formula: C8H10O4. Mole weight: 170.16. | |
| Penicillide | Penicillide is an acyl-CoA: cholesterol acyltransferase (ACAT) inhibitor produced by Penicillum asperosporum KY1635. The IC50 for inhibiting ACAT was 22.9 μmol/L. Synonyms: Vermixocin A; AS-186a; 11-hydroxy-3-[(1s)-1-hydroxy-3-methylbutyl]-4-methoxy-9-methyl-5h,7h-dibenzo[b,g][1,5]dioxocin-5-one. Grade: ≥95%. CAS No. 55303-92-9. Molecular formula: C21H24O6. Mole weight: 372.41. | |
| Penicillide (Vermixocin A, Antibiotic AS 186A, Antibiotic MC 140) | Plant growth inhibitor. Acyl-CoA-cholesterol acyltransferase (ACAT) inhibitor. Anticancer compound. Cytotoxic. Non-peptidic oxytocin receptor antagonist. Calpain inhibitor. Source:Isolated from Penicillium sp. Group: Biochemicals. Alternative Names: Vermixocin A, Antibiotic AS 186A, Antibiotic MC 140. Grades: Highly Purified. CAS No. 55303-92-9. Pack Sizes: 250ug, 1mg. Molecular Formula: C21H24O6, Molecular Weight: 372.4. US Biological Life Sciences. | Worldwide |
| Penicillin | It is produced by the strain of Cephalosporium aceemonium, C. salmosynnematum, Emericellopsis salmosynnemata. It has weak anti-gram-positive bacteria (activity against Staphylococcus aureus is only 1% of penicillin G) and anti-gram-negative bacteria activity, and can be broken down by penicillinase and cross-resistant to penicillin G. Synonyms: Penicillin N; Synnematin B; Cephalosporin N; Adicillin; Salmotin; SYNNEMATINB; Adicillinum; Synnematin N; (2S,5R,6R)-6-(5-Amino-5-carboxyvaleramido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptan-2-carbonsaeure; Cephalosphorin R; 6-N-((5-Amino-5-carboxy)pentanoyl)aminopenicillansaeure; (4-Amino-4-carboxybutyl)penicillin; NSC 113137; (D-4-Amino-4-carboxybutyl) penicillinic acid. Grade: 95%. CAS No. 525-94-0. Molecular formula: C14H21N3O6S. Mole weight: 359.40. | |
| penicillin amidase | This enzyme belongs to the family of hydrolases, those acting on carbon-nitrogen bonds other than peptide bonds, specifically in linear amides. The systematic name of this enzyme class is penicillin amidohydrolase. Other names in common use include penicillin acylase, benzylpenicillin acylase, novozym 217, semacylase, alpha-acylamino-beta-lactam acylhydrolase, and ampicillin acylase. This enzyme participates in penicillin and cephalosporin biosynthesis. Group: Enzymes. Synonyms: penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase. Enzyme Commission Number: EC 3.5.1.11. CAS No. 9014-6-6. Penicillin Amidase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4389; penicillin amidase; EC 3.5.1.11; 9014-06-6; penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase. Cat No: EXWM-4389. |  |
| Penicillin amidase, E. coli | Penicillin amidase (EC 3.5.1.11) (Penicillin acylase) is an enzyme that cleaves the acyl side chains of penicillins. Penicillin amidase can be used for the production of 6-aminopenicillanic acid. Penicillin amidase can also be used in the resolution of racemic mixtures, peptide synthesis, and synthesis of semi-synthetic β-lactam antibiotics [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PGA. CAS No. 9014-6-6. Pack Sizes: 100 mg; 250 mg. Product ID: HY-P2834. | |
| Penicillin Amidase from Escherichia coli | 5-10 units/mg protein. Group: Fluorescence/luminescence spectroscopy. | |
| Penicillinase | Penicillinase is a beta-lactamase. beta-lactamase enzymes inactivate beta-lactam antibiotics by hydrolyzing the peptide bond of the characteristic four-membered beta-lactam ring rendering the antibiotic ineffective [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9001-74-5. Pack Sizes: 5 mL. Product ID: HY-E70012. | |
| Penicillinase from Bacillus cereus | lyophilized, powder, white, ~13 U/mg. Group: Fluorescence/luminescence spectroscopy. | |
| Penicillin DF | Penicillin DF is used to characterize phenylacetate-CoA ligase from Penicillium chrysogenum. Group: Biochemicals. Grades: Highly Purified. CAS No. 4493-18-9. Pack Sizes: 10mg, 50mg. Molecular Formula: C14H22N2O4S, Molecular Weight: 314.399999999999. US Biological Life Sciences. | Worldwide |
| Penicillin F Sodium | It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It is an antibiotic. Synonyms: Sodium penicillin F; 2-Pentenylpenicillin sodium; Sodium 2-pentenylpenicillinate; Penicillin F sodium salt; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-((1-oxo-3-hexenyl)amino)-, monosodium salt, (2S-(2alpha,5alpha,6beta))-. CAS No. 525-86-0. Molecular formula: C14H19N2O4SNa. Mole weight: 334.37. | |
| Penicillin g | Penicillin g. Uses: Designed for use in research and industrial production. Additional or Alternative Names: PENICILLIN G K-SALT;PENICILLIN G POTASSIUM;PENICILLIN G POTASSIUM SALT;(5r,6r)-benzylpenicillin;(phenylmethyl)-penicilli;(phenylmethyl)penicillin;(phenylmethyl)-penicillinicaci;(phenylmethyl)penicillinicacid. Appearance: powder. CAS No. 61-33-6. Molecular formula: C16H18N2O4S. Mole weight: 334.39. Purity: 95%+. IUPACName: (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid. Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C. Density: 1.42g/cm³. ECNumber: 200-506-3. Product ID: ACM61336. Alfa Chemistry ISO 9001:2015 Certified. | |
| Penicillin G | Penicillin G is a β-lactam antibiotic produced by penicillin. Synonyms: Benzylpenicillin; Benzylpenicillinic Acid; Free Penicillin II. CAS No. 61-33-6. Molecular formula: C16H18N2O4S. Mole weight: 334.39. | |
| Penicillin g benzathine | Penicillin g benzathine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Penicillin G Benzathine Tetrahydrate; Penicillin G benzathine tetrahydrate. CAS No. 41372-02-5. Molecular formula: C48H64N6O12S2. Mole weight: 981.18. Purity: 0.96. IUPACName: N,N-dibenzylethane-1,2-diamine; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; tetra. Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C.C1=CC=C(C=C1)CNCCNCC2=CC=CC=C2.O.O.O.O. Product ID: ACM41372025. Alfa Chemistry ISO 9001:2015 Certified. | |
| Penicillin G benzathine | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Penicillin G benzathine | Penicillin G benzathine (Benzathine benzylpenicillin) is an antibiotic against many bacterial infections [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Benzathine benzylpenicillin. CAS No. 1538-09-6. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-N7139A. | |
| Penicillin G benzathine anhydrous | Penicillin G benzathine anhydrous. Group: Biochemicals. Alternative Names: Benzathine benzylpenicillin; Benzylpenicillin benzathine. Grades: Highly Purified. CAS No. 1538-09-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C16H20N2·2 (C16H18N2O4S). US Biological Life Sciences. | Worldwide |
| Penicillin G-[d7] N-ethylpiperidinium salt | Penicillin G-[d7] N-ethylpiperidinium salt is the labelled salt of Penicillin G, which is an impurity of penicilline. Synonyms: (2S-(2α,5α,6β))-3,3-Dimethyl-7-oxo-6-phenylacetyl-D7-amino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 1-ethyl-piperidinium; Benzylpenicilline-D7 N-ethylpiperidinium salt; Penicillin G-D7 N-ethylpiperidinium salt. Grade: 95% by HPLC; 98% atom D. CAS No. 1217445-37-8. Molecular formula: C23H26D7N3O4S. Mole weight: 454.63. | |
| Penicillin G-d7 N-ethylpiperidinium salt | analytical standard. Group: Application areas. | |
| Penicillin-g-p-methoxybenzyl ester sulfoxide | Penicillin-g-p-methoxybenzyl ester sulfoxide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: GEO;PENICILLIN-G-4-METHOXYBENZYL ESTER SULFOXIDE;PENICILLIN-G-P-METHOXYBENZYL ESTER SULFOXIDE. Product Category: Heterocyclic Organic Compound. CAS No. 53956-74-4. Molecular formula: C24H26N2O6S. Mole weight: 485.57. Product ID: ACM53956744. Alfa Chemistry ISO 9001:2015 Certified. | |
| Penicillin G potassium | Penicillin G potassium is a fast-acting penicillin family antibiotic. Penicillin G potassium can be used for the research of bacterial infections that affect the blood, heart, lungs, joints, and genital areas [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Benzylpenicillin potassium. CAS No. 113-98-4. Pack Sizes: 5 g; 10 g. Product ID: HY-17591. | |
| Penicillin G potassium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Penicillin G potassium salt | analytical standard. Group: Application areas. | |
| Penicillin G Potassium Salt | Penicillin G is a narrow spectrum antibiotic derived from Streptococcus pneumoniae. It is the drug of choice for groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridians group streptococci, and non-penicillinase producing staphylococcus. The potassium salt has been used to study murosomes of staphylococci and the penicillin-induced lysis of Streptococcus mutans. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium Salt; Penicillin G Potassium Salt; Benzylpenicillin Potassium; Cosmopen; Cristapen; Crytapen; Eskacillin; Falapen; Forpen; Hipercilina; Hyasorb; Hylenta; M-Cillin; Monopen; NSC 131815; Notaral; Pentid; Pentids; Potassium 6- (Phenylacetamido) penicillanate; Potassium Benzylpenicillin; Potassium Benzylpenicillinate; Potassium Penicillin G; Scotcil; Tabilin. Grades: Cell Culture Grade. CAS No. 113-98-4. Pack Sizes: 100g, 500g, 1Kg. US Biological Life Sciences. | Worldwide |
| Penicillin G potassium salt (Benzylpenicillin potassium salt) | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O4S. CAS No. 113-98-4. Prepack ID 23531529-25g. Molecular Weight 372.48. See USA prepack pricing. | |
| Penicillin G potassium (Standard) | Penicillin G (potassium) (Standard) is the analytical standard of Penicillin G (potassium). This product is intended for research and analytical applications. Penicillin G potassium is a fast-acting penicillin family antibiotic. Penicillin G potassium can be used for the research of bacterial infections that affect the blood, heart, lungs, joints, and genital areas [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 113-98-4. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17591R. | |
| Penicillin G procaine | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Penicillin G procaine hydrate | Penicillin G Procaine hydrate (PGP hydrate), a β-lactam antibiotic , is a crystalline complex produced by chemically combining penicillin G with procaine [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PGP hydrate. CAS No. 6130-64-9. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N7120. | |
| Penicillin G sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Penicillin G sodium salt | Penicillin G sodium salt is a typical β-lactam antibiotic. Uses: Scientific research. Group: Natural products. Alternative Names: Benzylpenicillin sodium salt. CAS No. 69-57-8. Pack Sizes: 100 mg. Product ID: HY-B1463. | |
| Penicillin G sodium salt | It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It has strong activity of anti-gram-positive bacteria and spirochetes, and has weak anti-gram-negative bacteria activity. It is widely used in clinical practice. Uses: Anti-bacterial agents. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6-(Phenylacetamido)penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Penicillin; Sodium Penicillin G; NSC 69877; NSC-69877; NSC69877; 7-NO2-ICA. Grade: 98%. CAS No. 69-57-8. Molecular formula: C16H17N2NaO4S. Mole weight: 356.37. | |
| Penicillin G sodium salt (Benzylpenicillin sodium salt) | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-5g. Molecular Weight 356.37. See USA prepack pricing. | |
| Penicillin G sodium salt (Benzylpenicillin sodium salt) | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-25g. Molecular Weight 356.37. See USA prepack pricing. | |
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